Synthesis and structure–activity relationships of second-generation hydroxamate botulinum neurotoxin a protease inhibitors

K Čapková, Y Yoneda, TJ Dickerson…

Index: Capkova, Katerina; Yoneda, Yoshiyuki; Dickerson, Tobin J.; Janda, Kim D. Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 23 p. 6463 - 6466

Full Text: HTML

Citation Number: 38

Abstract

Botulinum neurotoxins are the most toxic proteins currently known. Based on a recently identified potent lead structure, 2, 4-dichlorocinnamic acid hydroxamate, herein we report on the structure–activity relationship of a series of hydroxamate BoNT/A inhibitors. Among them, 2-bromo-4-chlorocinnamic acid hydroxamate, 2-methyl-4-chlorocinnamic acid hydroxamate, and 2-trifluoromethyl-4-chlorocinnamic acid hydroxamate displayed comparable inhibitory ...

Related Articles:

Synthesis and structure–activity relationships of N-aryl (indol-3-yl) glyoxamides as antitumor agents

[Marchand, Pascal; Antoine, Maud; Baut, Guillaume Le; Czech, Michael; Baasner, Silke; Guenther, Eckhard Bioorganic and Medicinal Chemistry, 2009 , vol. 17, # 18 p. 6715 - 6727]

More Articles...